Data / Medical devices / China / Shenzhen Xiangtong Co., Ltd.
Shenzhen Xiangtong Co., Ltd.: FDA-registered device maker in Dongguan Guangdong, China, 6 510(k) clearances
Shenzhen Xiangtong Co., Ltd. is registered with the FDA (registration 3018252381) in Dongguan Guangdong, China. It lists 1 device type. The FDA files 6 510(k) clearances under its listings, the newest dated December 8, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3018252381
- Address
- Room 101,301,701,801,Building 1,No. 110,Guanchang Road,Dalingshan Town, Dongguan Guangdong, China, 523800
- Owner or operator
- SHENZHEN XIANGTONG CO., LTD. (10088854)
- Roles
- Manufacturer
- First device listed
- October 17, 2023
- Registered through
- 2026
- Brand names listed
- Coloring Liquid, Glass Ceramic, X-Cera Zirconia Blanks, X-cera Pre-shaded Zirconia Blanks, XT Stain/Glaze
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powder, Porcelain | EIH | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 8, 2025 | K252789 | Glass Ceramic | EIH | Substantially Equivalent | Shenzhen Xiangtong Co., Ltd. | accessdata.fda.gov |
| March 27, 2023 | K223192 | XT Stain/Glaze | EIH | Substantially Equivalent | Shenzhen Xiangtong Co., Ltd. | accessdata.fda.gov |
| February 10, 2023 | K223194 | Glass Ceramic | EIH | Substantially Equivalent | Shenzhen Xiangtong Co., Ltd. | accessdata.fda.gov |
| June 29, 2022 | K220017 | Coloring Liquid | EIH | Substantially Equivalent | Dongguan Xiangtong Co., Ltd. | accessdata.fda.gov |
| December 10, 2020 | K202673 | X-cera Pre-shaded Zirconia Blanks | EIH | Substantially Equivalent | Dongguan Xiangtong Co., Ltd. | accessdata.fda.gov |
| March 29, 2016 | K153767 | X-cera Zirconia Blanks | EIH | Substantially Equivalent | Shenzhen Xiangtong Photoelectricity Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated December 8, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.